7133-16-6 Usage
Description
(Butylsulfanyl)cyclopentane is a chemical compound that features a cyclopentane ring with a butylsulfanyl group attached to it. (butylsulfanyl)cyclopentane is recognized for its unique structure and properties, which make it valuable in research and industrial applications. The butylsulfanyl group, a sulfur-containing substituent, provides reactivity and functional diversity to the molecule, making it useful in a variety of chemical reactions.
Uses
Used in Pharmaceutical Industry:
(Butylsulfanyl)cyclopentane is used as an intermediate in organic synthesis for the production of pharmaceuticals. Its unique structure and the reactivity of the butylsulfanyl group make it a valuable building block for creating more complex organic molecules, which can be further utilized in the development of new drugs.
Used in Agrochemical Industry:
(Butylsulfanyl)cyclopentane is also used as an intermediate in the synthesis of agrochemicals. (butylsulfanyl)cyclopentane's functional diversity and reactivity contribute to the development of new agrochemical products, such as pesticides and fertilizers, that can improve agricultural productivity and crop protection.
Used in Research and Development:
(Butylsulfanyl)cyclopentane serves as a key compound in research and development, particularly in the field of organic chemistry. Its unique structure and properties make it an ideal candidate for exploring new chemical reactions and synthesizing novel organic molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7133-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7133-16:
(6*7)+(5*1)+(4*3)+(3*3)+(2*1)+(1*6)=76
76 % 10 = 6
So 7133-16-6 is a valid CAS Registry Number.
7133-16-6Relevant articles and documents
Biotransformation of organic sulfides - VIII. A predictive model for sulfoxidation by Helminthosporium species NRRL 4671
Holland, Herbert L.,Brown, Frances M.,Lakshmaiah, Gingipalli,Larsen, Brett G.,Patel, Manish
, p. 683 - 697 (2007/10/03)
The fungus Helminthosporium species NRRL 4671 converts a wide range of prochiral sulfides to the corresponding chiral sulfoxides, the majority of which have (S) configuration at sulfur. The formation of a series of chiral cyclopentyl alkyl, cyclohexyl alkyl, benzyl alkyl, and methyl alkyl sulfoxides by biotransformation of the corresponding sulfides using Helminthosporium species is described. The analysis of over 90 such biotransformations has resulted in the development of a model based on restrictive-space descriptors that has been used to rationalize these reactions, and that is proposed as a predictor of the outcome of Helminthosporium-catalyzed sulfoxidations.
